A standardized comparison of commercially available prion decontamination reagents using the Standard Steel-Binding Assay

Journal of General Virology

Volumn 92, Issue 3, 2011, Pages 718-726

  Edgeworth, Julie Ann ^a   Sicilia, Anita ^a   Linehan, Jackie ^a   Brandner, Sebastian ^a   Jackson, Graham S ^a   Collinge, John ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

REAGENT;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; BINDING ASSAY; BIOASSAY; BRAIN HOMOGENATE; CONTROLLED STUDY; DISINFECTION; INSTRUMENT STERILIZATION; MOLECULAR DYNAMICS; MOUSE; NONHUMAN; PRION; PRION DISEASE; PRIORITY JOURNAL; SENSITIVITY ANALYSIS; STANDARD STEEL BINDING ASSAY; VIRAL CONTAMINATION; VIRUS INFECTIVITY; VIRUS TRANSMISSION;

ANIMALS; DECONTAMINATION; DISINFECTANTS; DISINFECTION; HUMANS; INFECTION CONTROL; MAMMALS; PRION DISEASES; PRIONS; STEEL; STERILIZATION;

BOS; BOVINAE; MAMMALIA;

EID: 79951799434     PISSN: 00221317     EISSN: 14652099     Source Type: Journal    
DOI: 10.1099/vir.0.027201-0     Document Type: Article

References (58)

1. Asante, E. A., Linehan, J. M., Desbruslais, M., Joiner, S., Gowland, I., Wood, A. L., Welch, J., Hill, A. F., Lloyd, S. E. & other authors (2002). BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein. EMBO J 21, 6358-6366. (Pubitemid 35448414)
2. Asante, E. A., Gowland, I., Grimshaw, A., Linehan, J. M., Smidak, M., Houghton, R., Osiguwa, O., Tomlinson, A., Joiner, S. & other authors (2009). Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins. J Gen Virol 90, 546-558.
3. Bernoulli, C., Siegfried, J., Baumgartner, G., Regli, F., Rabinowicz, T., Gajdusek, D. C. & Gibbs, C. J., Jr (1977). Danger of accidental person-to-person transmission of Creutzfeldt-Jakob disease by surgery. Lancet 1, 478-479. (Pubitemid 8045134)
4. Bramble, M. G. & Ironside, J. W. (2002). Creutzfeldt-Jakob disease: implications for gastroenterology. Gut 50, 888-890. (Pubitemid 34539056)
5. Bruce, M. E., McConnell, I., Will, R. G. & Ironside, J. W. (2001). Detection of variant Creutzfeldt-Jakob disease infectivity in extraneural tissues. Lancet 358, 208-209. (Pubitemid 32718547)
6. Bueler, H., Aguzzi, A., Sailer, A., Greiner, R. A., Autenried, P., Aguet, M. & Weissmann, C. (1993). Mice devoid of PrP are resistant to scrapie. Cell 73, 1339-1347. (Pubitemid 23201147)
7. Clewley, J. P., Kelly, C. M., Andrews, N., Vogliqi, K., Mallinson, G., Kaisar, M., Hilton, D. A., Ironside, J. W., Edwards, P. & other authors (2009). Prevalence of disease related prion protein in anonymous tonsil specimens in Britain: cross sectional opportunistic survey. BMJ 338, b1442.
8. Collinge, J. (2001). Prion diseases of humans and animals: their causes and molecular basis. Annu Rev Neurosci 24, 519-550.
9. Collinge, J. & Clarke, A. R. (2007). A general model of prion strains and their pathogenicity. Science 318, 930-936. (Pubitemid 350098981)
10. Collins, S., Law, M. G., Fletcher, A., Boyd, A., Kaldor, J. & Masters, C. L. (1999). Surgical treatment and risk of sporadic Creutzfeldt-Jakob disease: a case-control study. Lancet 353, 693-697. (Pubitemid 29103801)
11. Cronier, S., Gros, N., Tattum, M. H., Jackson, G. S., Clarke, A. R., Collinge, J. & Wadsworth, J. D. (2008). Detection and characterization of proteinase K-sensitive disease-related prion protein with thermolysin. Biochem J 416, 297-305.
12. Davanipour, Z., Alter, M., Sobel, E. & Callahan, M. (1985). Sheep consumption: a possible source of spongiform encephalopathy in humans. Neuroepidemiology 4, 240-249. (Pubitemid 16108136)
13. de Pedro-Cuesta, J., Mahillo-Fernandez, I., Rabano, A., Calero, M., Cruz, M., Siden, A., Laursen, H., Falkenhorst, G. & Molbak, K. (2010). Nosocomial transmission of sporadic Creutzfeldt-Jakob disease: results from a risk-based assessment of surgical interventions. J Neurol Neurosurg Psychiatry (14 June; Epub ahead of print).
14. Edgeworth, J. A., Jackson, G. S., Clarke, A. R., Weissmann, C. & Collinge, J. (2009). Highly sensitive, quantitative cell-based assay for prions adsorbed to solid surfaces. Proc Natl Acad Sci U S A 106, 3479-3483.
15. Fichet, G., Comoy, E., Duval, C., Antloga, K., Dehen, C., Charbonnier, A., McDonnell, G., Brown, P., Lasmezas, C. I. & Deslys, J. P. (2004). Novel methods for disinfection of prion-contaminated medical devices. Lancet 364, 521-526. (Pubitemid 39070412)
16. Fischer, M., Rulicke, T., Raeber, A., Sailer, A., Moser, M., Oesch, B., Brandner, S., Aguzzi, A. & Weissmann, C. (1996). Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie. EMBO J 15, 1255-1264. (Pubitemid 26093461)
17. Flechsig, E., Hegyi, I., Enari, M., Schwarz, P., Collinge, J. & Weissmann, C. (2001). Transmission of scrapie by steel-surface-bound prions. Mol Med 7, 679-684. (Pubitemid 33070982)
18. Frosh, A., Smith, L. C., Jackson, C. J., Linehan, J., Brandner, S., Wadsworth, J. D. & Collinge, J. (2004). Analysis of 2000 consecutive UK tonsillectomy specimens for disease-related prion protein. Lancet 364, 1260-1262.
19. Gibbs, C. J., Jr, Asher, D. M., Kobrine, A., Amyx, H. L., Sulima, M. P. & Gajdusek, D. C. (1994). Transmission of Creutzfeldt-Jakob disease to a chimpanzee by electrodes contaminated during neurosurgery. J Neurol Neurosurg Psychiatry 57, 757-758. (Pubitemid 24182968)
20. Giles, K., Glidden, D. V., Beckwith, R., Seoanes, R., Peretz, D., DeArmond, S. J. & Prusiner, S. B. (2008). Resistance of bovine spongiform encephalopathy (BSE) prions to inactivation. PLoS Pathog 4, e1000206.
21. Glatzel, M., Abela, E., Maissen, M. & Aguzzi, A. (2003). Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease. N Engl J Med 349, 1812-1820. (Pubitemid 37362957)
22. Griffith, J. S. (1967). Self replication and scrapie. Nature 215, 1043-1044.
23. Head, M. W., Ritchie, D., Smith, N., McLoughlin, V., Nailon, W., Samad, S., Masson, S., Bishop, M., McCardle, L. & Ironside, J. W. (2004). Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study. Am J Pathol 164, 143-153. (Pubitemid 38364599)
24. Hernandez-Palazon, J., Martinez-Lage, J. F., Tortosa, J. A. & Garcia-Cayuela, J. M. (1998). Anaesthetic management in patients suspected of, or at risk of, having Creutzfeldt-Jakob disease. Br J Anaesth 80, 516-518. (Pubitemid 28171383)
25. Hill, A. F., Desbruslais, M., Joiner, S., Sidle, K. C., Gowland, I., Collinge, J., Doey, L. J. & Lantos, P. (1997). The same prion strain causes vCJD and BSE. Nature 389, 448-450, 526.
26. Hill, A. F., Butterworth, R. J., Joiner, S., Jackson, G. S., Rossor, M. N., Thomas, D. J., Frosh, A., Tolley, N., Bell, J. E. & other authors (1999). Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples. Lancet 353, 183-189.
27. Hilton, D. A., Ghani, A. C., Conyers, L., Edwards, P., McCardle, L., Ritchie, D., Penney, M., Hegazy, D. & Ironside, J. W. (2004). Prevalence of lymphoreticular prion protein accumulation in UK tissue samples. J Pathol 203, 733-739. (Pubitemid 38961558)
28. HPA Press Office (2009). vCJD abnormal prion protein found in a patient with haemophilia at post mortem.
29. Jackson, G. S.,McKintosh, E., Flechsig, E., Prodromidou, K., Hirsch, P., Linehan, J., Brandner, S., Clarke, A. R., Weissmann, C. & Collinge, J. (2005). An enzyme-detergent method for effective prion decontamination of surgical steel. J Gen Virol 86, 869-878. (Pubitemid 40331269)
30. Joiner, S., Linehan, J., Brandner, S., Wadsworth, J. D. & Collinge, J. (2002). Irregular presence of abnormal prion protein in appendix in variant Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry 73, 597-598.
31. Joiner, S., Linehan, J., Brandner, S., Wadsworth, J. D. & Collinge, J. (2005). High Levels of disease related prion protein in the ileum in variant Creutzfeldt-Jakob disease. Gut 54, 1506-1508.
32. Klohn, P. C., Stoltze, L., Flechsig, E., Enari, M. & Weissmann, C. (2003). A quantitative, highly sensitive cell-based infectivity assay for mouse scrapie prions. Proc Natl Acad Sci U S A 100, 11666-11671. (Pubitemid 37205992)
33. Lemmer, K., Mielke, M., Kratzel, C., Joncic, M., Oezel, M., Pauli, G. & Beekes, M. (2008). Decontamination of surgical instruments from prions. II. In vivo findings with a model system for testing the removal of scrapie infectivity from steel surfaces. J Gen Virol 89, 348-358.
34. Llewelyn, C. A., Hewitt, P. E., Knight, R. S., Amar, K., Cousens, S., Mackenzie, J. & Will, R. G. (2004). Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion. Lancet 363, 417-421. (Pubitemid 38210057)
35. Mahillo-Fernandez, I., Pedro-Cuesta, J., Bleda, M. J., Cruz, M., Molbak, K., Laursen, H., Falkenhorst, G., Martinez-Martin, P. & Siden, A. (2008). Surgery and risk of sporadic Creutzfeldt-Jakob disease in Denmark and Sweden: registry-based case-control studies. Neuroepidemiology 31, 229-240.
36. Minatogawa, T. & Kumoi, T. (1999). Problems in utility and safety of otological allografts. Transplant Proc 31, 2036-2037. (Pubitemid 29376521)
37. Murdoch, H., Taylor, D., Dickinson, J., Walker, J. T., Perrett, D., Raven, N. D. & Sutton, J. M. (2006). Surface decontamination of surgical instruments: an ongoing dilemma. J Hosp Infect 63, 432-438. (Pubitemid 44040844)
38. Notari, S., Moleres, F. J., Hunter, S. B., Belay, E. D., Schonberger, L. B., Cali, I., Parchi, P., Shieh, W. J., Brown, P. & other authors (2010). Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States. PLoS ONE 5, e8765.
39. Peden, A. H., Head, M. W., Ritchie, D. L., Bell, J. E. & Ironside, J. W. (2004). Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient. Lancet 364, 527-529. (Pubitemid 39070413)
40. Peden, A., McCardle, L., Head, M. W., Love, S., Ward, H. J., Cousens, S. N., Keeling, D. M., Millar, C. M., Hill, F. G. & Ironside, J. W. (2010). Variant CJD infection in the spleen of a neurologically asymptomatic UK adult patient with haemophilia. Haemophilia 16, 296-304.
41. Peretz, D., Supattapone, S., Giles, K., Vergara, J., Freyman, Y., Lessard, P., Safar, J. G., Glidden, D. V., McCulloch, C. & other authors (2006). Inactivation of prions by acidic sodium dodecyl sulfate. J Virol 80, 322-331.
42. Prusiner, S. B. (1982). Novel proteinaceous infectious particles cause scrapie. Science 216, 136-144.
43. Prusiner, S. B., Groth, D. F., McKinley, M. P., Cochran, S. P., Bowman, K. & Kasper, K. C. (1981). Thiocyanate and hydroxyl ions inactivate the scrapie agent. Proc Natl Acad Sci U S A 78, 4606-4610.
44. Rutala, W. A. & Weber, D. J. (2001). Creutzfeldt-Jakob disease: recommendations for disinfection and sterilization. Clin Infect Dis 32, 1348-1356. (Pubitemid 32405909)
45. SEAC (2006). Position statement on methods to evaluate decontamination technologies for surgical instruments. http://www.seac.gov.uk/statements/ statement310806.htm
46. Smith, A., Dickson, M., Aitken, J. & Bagg, J. (2002). Contaminated dental instruments. J Hosp Infect 51, 233-235. (Pubitemid 38001897)
47. Somerville, R. A., Oberthur, R. C., Havekost, U., MacDonald, F., Taylor, D. M. & Dickinson, A. G. (2002). Characterization of thermodynamic diversity between transmissible spongiform encephalopathy agent strains and its theoretical implications. J Biol Chem 277, 11084-11089. (Pubitemid 34952868)
48. Taylor, D. M. (1991). Inactivation of the unconventional agents of scrapie, bovine spongiform encephalopathy and Creutzfeldt-Jakob disease. J Hosp Infect 18, 141-146 (Suppl. A).
49. Taylor, D. M., Fernie, K., McConnell, I. & Steele, P. J. (1998). Observations on thermostable subpopulations of the unconventional agents that cause transmissible degenerative encephalopathies. Vet Microbiol 64, 33-38. (Pubitemid 28556941)
50. Taylor, D. M., Fernie, K., McConnell, I. & Steele, P. J. (1999). Survival of scrapie agent after exposure to sodium dodecyl sulphate and heat. Vet Microbiol 67, 13-16. (Pubitemid 29243837)
51. Wadsworth, J. D., Joiner, S., Hill, A. F., Campbell, T. A., Desbruslais, M., Luthert, P. J. & Collinge, J. (2001). Tissue distribution of protease resistant prion protein in variant CJD using a highly sensitive immunoblotting assay. Lancet 358, 171-180.
52. Wadsworth, J. D., Joiner, S., Fox, K., Linehan, J., Desbruslais, M., Brandner, S., Asante, E. A. & Collinge, J. (2007). Prion infectivity in variant Creutzfeldt-Jakob disease rectum. Gut 56, 90-94.
53. Walker, J. T., Dickinson, J., Sutton, J. M., Raven, N. D. & Marsh, P. D. (2007). Cleanability of dental instruments - implications of residual protein and risks from Creutzfeldt-Jakob disease. Br Dent J 203, 395-401.
54. Ward, H. J., Everington, D., Croes, E. A., Alperovitch, A., Delasnerie-Laupretre, N., Zerr, I., Poser, S. & van Duijn, C. M. (2002). Sporadic Creutzfeldt-Jakob disease and surgery: a case-control study using community controls. Neurology 59, 543-548. (Pubitemid 34919987)
55. WHO (1999). WHO Infection Control Guidelines for Transmissible Spongiform Encephalopathies. Geneva: WHO.
56. Wroe, S. J., Pal, S., Siddique, D., Hyare, H., Macfarlane, R., Joiner, S., Linehan, J., Brandner, S., Wadsworth, J. D. & other authors (2006). Clinical presentation and pre-mortem diagnosis of variant Creutzfeldt-Jakob disease associated with blood transfusion: a case report. Lancet 368, 2061-2067.
57. Yan, Z. X., Stitz, L., Heeg, P., Pfaff, E. & Roth, K. (2004). Infectivity of prion protein bound to stainless steel wires: a model for testing decontamination procedures for transmissible spongiform encephalopathies. Infect Control Hosp Epidemiol 25, 280-283. (Pubitemid 38524902)
58. Zobeley, E., Flechsig, E., Cozzio, A., Masato, E. & Weissmann, C. (1999). Infectivity of scrapie prions bound to a stainless steel surface. Mol Med 5, 240-243. (Pubitemid 29279752)